A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4555



Internal ID15549276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:152990418..152999515hg38UCSC Ensembl
Outerchr4:153911570..153920667hg19UCSC Ensembl
Outerchr4:154131020..154140117hg18UCSC Ensembl
Outerchr4:154269175..154278272hg17UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg385410
hg195410
hg185410
hg175410
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8014
SamplesNA12156
Known Genes
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nsv4555
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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